Korean J Physiol Pharmacol.
2000 Apr;4(2):99-104.
Differential effects of nitric oxide synthase inhibitors in rats
- Affiliations
-
- 1Department of Pharmacology, College of Pharmacy, Chung Ang
University, 221 Heuksuk-dong, Dongjak-gu, Seoul, South Korea.
Abstract
- We investigated the action of NOS inhibitors on NOS in rats. Both of
nitric oxide synthase inhibitors, NG-monomethyl-L-arginine (L-NMMA, 3
micrometer) or NG-nitro-L-arginine methylester (L-NAME, 30 micrometer), augmented
phenylephrine (PE, 10-7 M)-induced contraction which was inhibited by
acetylcholine (ACh) in rat thoracic aorta. This augmentation by L-NAME
or L-NMMA was attenuated with the treatment of NO precursor, arginine.
ACh, however, decreased the augmentation induced by L-NMMA, but not by
L-NAME. Superoxide dismutase (SOD, 50 u/ml) potentiated an inhibitory
effect of ACh on the PE (10-7 M)-induced contraction. It has been known
that platelet activating factor itself induces iNOS. Platelet
activating factor (PAF, 10-7 M) inhibited PE (10-7 M)-induced
contraction. Pretreatment with L-NMMA (30 mM) or L-NAME (30 mM)
significantly blocked the inhibitory action of PAF on PE-induced
contraction. L-NMMA (100 mM) or L-NAME (100 mM) reduced nerve
conduction velocity (NCV) relevant to nNOS in rat sciatic nerve. ACh
attenuated the reduction of NCV by L-NMMA-, but not by L-NAME-induced
reduction of NCV. These results suggest that L-NMMA and/or L-NAME have
different action on three types of NOS in rats.